WO2007149873A3 - Inhibiteurs du canal potassique kv1.5 - Google Patents

Inhibiteurs du canal potassique kv1.5 Download PDF

Info

Publication number
WO2007149873A3
WO2007149873A3 PCT/US2007/071586 US2007071586W WO2007149873A3 WO 2007149873 A3 WO2007149873 A3 WO 2007149873A3 US 2007071586 W US2007071586 W US 2007071586W WO 2007149873 A3 WO2007149873 A3 WO 2007149873A3
Authority
WO
WIPO (PCT)
Prior art keywords
potassium channel
channel inhibitors
present
selective
atrial
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2007/071586
Other languages
English (en)
Other versions
WO2007149873A2 (fr
Inventor
John Michael Janusz
Shengde Wu
Neil T Fairweather
Wenlin Lee
Benjamin E Blass
Andrew J Fluxe
Stephen J Hodson
James M Ii Ridgeway
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wyeth LLC
Original Assignee
Wyeth LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wyeth LLC filed Critical Wyeth LLC
Priority to AU2007260984A priority Critical patent/AU2007260984A1/en
Priority to JP2009516685A priority patent/JP2009541342A/ja
Priority to CA002654262A priority patent/CA2654262A1/fr
Priority to EP07798772A priority patent/EP2035420A2/fr
Priority to MX2008016273A priority patent/MX2008016273A/es
Publication of WO2007149873A2 publication Critical patent/WO2007149873A2/fr
Publication of WO2007149873A3 publication Critical patent/WO2007149873A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10—Spiro-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Cardiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

la présente invention concerne des 4-oxo-1,3,8-triaza-spiro[4.5]décanes convenant comme inhibiteurs du canal potassique Kv1.5 du fait qu'ils exercent une activité anti-arythmique à sélectivité auriculaire. De plus, cette invention concerne des compositions et une méthode de traitement anti-arythmie à sélectivité auriculaire.
PCT/US2007/071586 2006-06-20 2007-06-19 Inhibiteurs du canal potassique kv1.5 Ceased WO2007149873A2 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
AU2007260984A AU2007260984A1 (en) 2006-06-20 2007-06-19 Kv1.5 potassium channel inhibitors
JP2009516685A JP2009541342A (ja) 2006-06-20 2007-06-19 Ｋｖ１．５カリウムチャネル阻害剤
CA002654262A CA2654262A1 (fr) 2006-06-20 2007-06-19 Inhibiteurs du canal potassique kv1.5
EP07798772A EP2035420A2 (fr) 2006-06-20 2007-06-19 Inhibiteurs du canal potassique kv1.5
MX2008016273A MX2008016273A (es) 2006-06-20 2007-06-19 Inhibidores de canal de potasio kv1.5.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US81506606P 2006-06-20 2006-06-20
US60/815,066 2006-06-20

Publications (2)

Publication Number Publication Date
WO2007149873A2 WO2007149873A2 (fr) 2007-12-27
WO2007149873A3 true WO2007149873A3 (fr) 2008-03-06

Family

ID=38799301

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2007/071586 Ceased WO2007149873A2 (fr) 2006-06-20 2007-06-19 Inhibiteurs du canal potassique kv1.5

Country Status (12)

Country Link
US (1) US20070299072A1 (fr)
EP (1) EP2035420A2 (fr)
JP (1) JP2009541342A (fr)
CN (1) CN101472924A (fr)
AR (1) AR061522A1 (fr)
AU (1) AU2007260984A1 (fr)
CA (1) CA2654262A1 (fr)
CL (1) CL2007001795A1 (fr)
MX (1) MX2008016273A (fr)
PE (1) PE20080207A1 (fr)
TW (1) TW200813053A (fr)
WO (1) WO2007149873A2 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2008338368A1 (en) * 2007-12-19 2009-06-25 Wyeth Llc 4-imidazolidinones as Kv1.5 potassium channel inhibitors
BRPI0821394A2 (pt) * 2007-12-19 2015-06-16 Wyeth Llc 4-imidazolidinonas como inibidores de canal de potássio kv1.5
US20110166124A1 (en) * 2008-07-23 2011-07-07 Mccormick Kevin D Tricyclic spirocycle derivatives and methods of use
JP5671453B2 (ja) * 2009-04-28 2015-02-18 中外製薬株式会社 スピロイミダゾロン誘導体
KR102168738B1 (ko) 2012-12-10 2020-10-22 추가이 세이야쿠 가부시키가이샤 히단토인 유도체
KR102266021B1 (ko) * 2014-06-09 2021-06-16 추가이 세이야쿠 가부시키가이샤 히단토인 유도체 함유 의약 조성물
WO2021097117A2 (fr) * 2019-11-13 2021-05-20 Temple University-Of The Commonwealth System Of Higher Education Nouvelles lactones fonctionnalisées constituant des modulateurs du récepteur de la 5-hydroxytryptamine 7 et leur procédé d'utilisation
JP2023537994A (ja) * 2020-08-11 2023-09-06 ボード オブ トラスティーズ オブ ミシガン ステイト ユニバーシティ プロテアソームエンハンサーおよびその使用

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001040231A1 (fr) * 1999-12-06 2001-06-07 Bristol-Myers Squibb Company Dihydropyrimidines heterocycliques utiles en tant qu'inhibiteurs des canaux potassium
WO2005058890A2 (fr) * 2003-12-12 2005-06-30 Solvay Pharmaceuticals Gmbh Derives d'hydronopol utilises comme agonistes des recepteurs orl1 humains

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3155670A (en) * 1962-06-22 1964-11-03 Res Lab Dr C Janssen N V 1-oxo-2, 4, 8, triaza-spiro (4, 5) decanes
US3155669A (en) * 1962-06-22 1964-11-03 Res Lab Dr C Janssen N V 2, 4, 8-triaza-spiro (4, 5) dec-2-enes
US3839341A (en) * 1966-06-13 1974-10-01 Fmc Corp Substituted 1,3,8-triazaspiro(4.5)decanes
US3901898A (en) * 1971-04-15 1975-08-26 Sumitomo Chemical Co 8-aroylalkyl-1,3,8-triazaspiro (4,5)+0 decanes
US4656280A (en) * 1984-03-07 1987-04-07 E. I. Du Pont De Nemours And Company Radioiodinated dopamine receptor ligand
US4707484A (en) * 1986-11-25 1987-11-17 Hoffmann-La Roche Inc. Substituted piperidinomethylindolone and cyclopent(b)indolone derivatives
US4876260A (en) * 1987-10-28 1989-10-24 State Of Israel, Israel Institute Of Biological Research Oxathiolanes
US5244902A (en) * 1989-08-21 1993-09-14 Beth Israel Hospital Association Topical application of spiperone or derivatives thereof for treatment of pathological conditions associated with immune responses
ES2170446T3 (es) * 1997-12-05 2002-08-01 Hoffmann La Roche Derivados de 1,3,8-triaza-espiro(4,5)decan-4-ona.
US6277991B1 (en) * 1998-05-18 2001-08-21 Novo Nordisk A/S 1,3,8-triazaspiro[4.5]decanones with high affinity for opioid receptor subtypes
US6262066B1 (en) * 1998-07-27 2001-07-17 Schering Corporation High affinity ligands for nociceptin receptor ORL-1
US6482829B2 (en) * 2000-06-08 2002-11-19 Hoffmann-La Roche Inc. Substituted heterocyclic siprodecane compound active as an antagonist of neurokinin 1 receptor
KR100798161B1 (ko) * 2003-10-23 2008-01-28 에프. 호프만-라 로슈 아게 신경병적 또는 신경정신병적 장애의 치료에서 ｇｌｙｔ-1저해제로서 사용하기 위한 트라이아자-스피로피페리딘유도체

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001040231A1 (fr) * 1999-12-06 2001-06-07 Bristol-Myers Squibb Company Dihydropyrimidines heterocycliques utiles en tant qu'inhibiteurs des canaux potassium
WO2005058890A2 (fr) * 2003-12-12 2005-06-30 Solvay Pharmaceuticals Gmbh Derives d'hydronopol utilises comme agonistes des recepteurs orl1 humains

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DU LÜ-PEI ET AL: "The pharmacophore hypotheses of I(Kr) potassium channel blockers: novel class III antiarrhythmic agents.", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 20 SEP 2004, vol. 14, no. 18, 20 September 2004 (2004-09-20), pages 4771 - 4777, XP002462369, ISSN: 0960-894X *

Also Published As

Publication number Publication date
CL2007001795A1 (es) 2008-01-18
AR061522A1 (es) 2008-09-03
JP2009541342A (ja) 2009-11-26
AU2007260984A1 (en) 2007-12-27
EP2035420A2 (fr) 2009-03-18
MX2008016273A (es) 2009-01-15
CA2654262A1 (fr) 2007-12-27
US20070299072A1 (en) 2007-12-27
WO2007149873A2 (fr) 2007-12-27
TW200813053A (en) 2008-03-16
CN101472924A (zh) 2009-07-01
PE20080207A1 (es) 2008-05-08

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